Search results for "Mesityl oxide"
showing 3 items of 3 documents
Photo-assisted degradation of 2-propanol in gas–solid regime by using TiO2 impregnated with heteropolyacid H3PW12O40
2009
Abstract Commercial and home prepared TiO2 samples impregnated with tungstophosphoric acid (H3PW12O40) were used for the photo-assisted degradation of 2-propanol in gas–solid regime. The characterization results evidenced a good coverage of the polyoxometalate (POM) onto the surface of TiO2 along with a marginal effect of the presence of the POM on the specific surface area, morphology and cristallinity of the samples. Propene was the main intermediate product revealed in 2-propanol photocatalytic degradation by using as photocatalysts the samples containing the POM, whereas propanone was mainly obtained when the photocatalysts was bare TiO2, both commercial or home prepared. Acetaldehyde w…
Direct synthesis of methyl isobutyl ketone in gas-phase reaction over palladium-loaded hydroxyapatite
2005
Several compositions of palladium-loaded calcium hydroxyapatite Pd(x)/CaHAp were prepared and characterized by XRD, IR, and UV–visible spectroscopy and temperature-programmed reduction (TPR). The acid–base properties of the samples were studied with the use of butan-2-ol conversion and IR spectroscopy coupled with lutidine adsorption/desorption. Calcium hydroxyapatite bears Lewis acid sites of moderate strength and a limited number of Bronsted acid sites, which produce butenes by dehydration. The selectivity of the dehydrogenation reaction (formation of methyl ethyl ketone) is very limited in the absence of oxygen but indicates the existence on the surface of phosphate of basic sites that a…
Reduction and catalytic behaviour of heterobimetallic copper–lanthanide oxides
2008
Abstract The reduction of the heterobimetallic copper–lanthanide oxides 2CuO·CeO2 and 3CuO·Ln2CuO4 (Ln = La, Pr, Nd) was studied by H2-TG/DTA and H2-TPR. All systems exhibit two main reduction steps accompanied by mass losses in the temperature range 20–1000 °C. The first step was attributed to CuO reduction, whereas the second step is due either to copper reduction in the Ln2CuO4 phase with the concomitant formation of Ln2O3 or to the surface reduction of CeO2. The products were characterized by XRD, SEM, EDX, and BET techniques and are better described as supported copper type materials. They were active for the mesityl oxide (4-methyl-2-penten-2-one) gas phase hydrogenation.